Department of Mathematics, University of Liège, Grande Traverse 12, B37, Liège 4000, Belgium.
Clin Trials. 2009 Oct;6(5):403-15. doi: 10.1177/1740774509344777. Epub 2009 Sep 8.
Structural mean models can be used to estimate treatment efficacy when drug exposure varies. We applied structural mean model to evaluate the clinical benefits of a proton pump inhibitor prescribed to be taken as needed to alleviate epigastric pain. We also investigated a new diagnostic approach to evaluate model assumptions.
All patients were suffering from nonerosive reflux disease or functional ulcer-like dyspepsia and were prescribed a proton pump inhibitor to be taken as needed for relief of epigastric pain. The primary endpoint was a score variable that expresses the magnitude of gastro-intestinal symptoms at 8 weeks after randomization. We developed linear and loglinear versions of the structural mean models to derive an unbiased estimator of the reduction in symptom score as a function of exposure to the test drug. Semi-parametric models based on splines and corresponding simultaneous confidence bands identified the presence of potential interactions between drug exposure and baseline covariates.
The on-demand dosing regimen generated a wide range of drug exposure. Application of SMM showed that the potential treatment-induced reduction in symptom score was much greater than the average treatment reduction observed in this population of patients. Our diagnostic tool was useful for detecting the interaction between drug exposure and baseline covariates.
Analysis could only be performed over the first 2 months after randomization because, afterwards, many patients dropped out from the placebo group.
The structural mean model approach allows one to estimate treatment efficacy in the presence of variable drug exposure. Similar results were obtained using linear and loglinear structural mean model.
结构均值模型可用于估计药物暴露量变化时的治疗效果。我们应用结构均值模型评估质子泵抑制剂按需缓解上腹痛的临床获益。我们还探索了一种新的诊断方法来评估模型假设。
所有患者均患有非糜烂性反流病或功能性溃疡样消化不良,并被开具质子泵抑制剂,按需服用以缓解上腹痛。主要终点是一个评分变量,表示随机分组后 8 周时胃肠症状的严重程度。我们开发了线性和对数线性结构均值模型,以推导出作为药物暴露函数的症状评分降低的无偏估计量。基于样条的半参数模型和相应的同时置信带确定了药物暴露与基线协变量之间潜在交互作用的存在。
按需给药方案产生了广泛的药物暴露。应用 SMM 表明,潜在的治疗引起的症状评分降低幅度明显大于该患者人群中观察到的平均治疗降低幅度。我们的诊断工具对于检测药物暴露与基线协变量之间的相互作用很有用。
由于之后许多安慰剂组患者退出,因此只能在随机分组后 2 个月内进行分析。
结构均值模型方法可在存在可变药物暴露的情况下估计治疗效果。线性和对数线性结构均值模型均得到了类似的结果。